Mystery surrounding DYT2 dystonia now solved: HPCA mutations identified in DYT2-like family.

Subjects

Subjects :

Humans
Dystonia genetics
Genes, Recessive genetics
Hippocalcin genetics
Mutation genetics

Details

Language :

English

ISSN :

1531-8257

Volume :

30

Issue :

8

Database :

MEDLINE

Journal :

Movement disorders : official journal of the Movement Disorder Society

Publication Type :

Academic Journal

Accession number :

26095160

Full Text :

https://doi.org/10.1002/mds.26288